Phenotypic Plasticity and Fitness in Egg Parasitoids

FORUM

Phenotypic Plasticity and Fitness in Egg Parasitoids

G

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Horticultural Research and Development Centre, Agriculture and Agri-Food Canada, 430 Boulevard Gouin, St-Jean-sur-Richelieu, Qc, J3B 3E6 Canada; Department of Natural Resource Sciences (Entomology), Macdonald

Campus of McGill Univ, 21111 Lakeshore Road, Ste-Anne-de-Bellevue, Qc, H9X 3V9 Canada Edited by Fernando L Cônsoli – ESALQ/USP

Neotropical Entomology 39(4):457-463 (2010)

ABSTRACT - Several proxies can be used to estimate the fi tness of egg parasitoids: size, longevity, fecundity, mating ability and vagility. All these proxies are positively correlated with the lifetime fi tness gain of an individual. However, the phenotypic plasticity, which is the ability of a genotype to produce distinct phenotypes depending on environmental conditions, may alter the value of these proxies. Host related factors (host species and quality), competition and duration of development will infl uence the proxies expressed by a given phenotype. When the phenotype is modifi ed by the temperature at which an individual develops, the resulting phenotype will vary based on the life history strategy of the parasitoid. While in koinobiont species an increase in size is positively correlated with longevity and fecundity, the reverse occurs with idiobiont parasitoids. Using size as a proxy could thus be misleading depending on the factors that infl uence the size of the adult.

KEY WORDS: Fitness, proxy, reproduction, longevity, phenotype

Most optimality models are based on the assumption that organisms optimize some physiological or behavioral characteristics in order to maximize their lifetime fi tness (Stephens & Krebs 1986). Fitness, defi ned here as the success of an individual in passing on copies of its genes to future generations (Bolhuis & Giraldeau 2005), is therefore used as a measure of success and any change in the morphology, physiology or behavior of an animal that increases its lifetime fi tness is expected to be positively selected. This concept is central in behavioral ecology and both direct fi tness and inclusive fi tness are recognized. Direct fi tness refers to the fi tness gained by an individual through the production of its own offspring while inclusive fi tness refers to the sum of the direct fi tness plus the indirect fi tness gained by the reproduction of nondescendant relatives (Krebs & Davies 1997).

Insect parasitoids are good organisms to test hypothesis in behavioral ecology as the expression of behaviors associated with host localization and parasitization are directly linked to a gain in fi tness. Indeed, fi nding and successfully parasitizing a host results in additional progeny and therefore in an increase in fi tness (Godfray 1994). Another research area where measures of fi tness are used for parasitoids is applied ecology and in particular biological control (Roitberg et al 2001). When comparing different species or genotypes within a species for their potential in biological control programs, measures of fi tness can be used to assess their capacity to multiply and control a targeted pest.

However, measuring directly fi tness is a diffi cult and time-consuming process. One would have to measure the relative performance of genotypes and quantify their representation

in a population over several generations (Hoffman 1994). In general, proxies that give absolute values, such as size, longevity, fecundity etc., are used to approximate the fi tness of an individual. The different proxies that can be used for parasitoids along with their advantages and limitations have been discussed by Roitberg et al (2001). In this paper I would like to concentrate on egg parasitoids and discuss how the phenotypic plasticity found in these organisms infl uences their fi tness.

Egg Parasitoids

these characteristics result in diffi culties when it comes to use these insects in laboratory tests, they also open opportunities such a measuring the lifetime fecundity of females in less than a week.

Another characteristic of egg parasitoids is that most species display structured populations and often intense sib-mating at the emergence site, although some off-patch mating occurs (Martel & Boivin 2007). Such mating structure infl uences the relative importance of dispersion and insemination capacity of males in their estimation of fi tness.

Which Proxies Are Valid in Egg Parasitoids?

Roitberg et al (2001) have identifi ed ten fi tness proxies of importance for parasitoids. Of these, fi ve are especially relevant for egg parasitoids: size, longevity, fecundity, mating ability and vagility. The other proxies proposed by Roitberg et al (2001) also apply to egg parasitoids, but in most cases the biology or ecology of egg parasitoids make them poor proxies for fi tness. These poor proxies are: 1) Progeny survival is certainly important for larval and pupal parasitoids where the host immune system must be overcome or where hyperparasitoids are a major source of mortality. In egg parasitoids neither occur and only mortality due to competition following superparasitism could occur; 2) Developmental rate has an impact on the population dynamics of most parasitoid species. However, the development of most egg parasitoid species lasts 8 to 10 days and the observed variability in emergence is rather low (Doyon & Boivin 2006); 3) Sex ratio is considered as a weighting proxy when used in conjunction with realised fecundity, but it has no value as an absolute measure (Roitberg et al 2001); 4) Host acquisition measures the ability to fi nd, overcome and parasitize hosts. Because host eggs are immobile and defenceless, unless defended by the ovipositing female as in several species of Scelionidae (Waage 1982), vagility is more important as a measure of the capacity of egg parasitoids to fi nd and parasitize hosts; 5) Finally, oviposition propensity measures the tendency to accept hosts (Bourchier & Smith 1996). It is diffi cult to measure and is linked to host preference.

The Proxies Adapted to Egg Parasitoids

Size is considered as a good indicator of fi tness although it has no direct relation with fi tness. However, most other proxies are infl uenced by the size of an individual and in most cases a positive relationship is found (West et al 1996, Nicol & Mackauer 1999) (but see the section on phenotypic variability). In several species of Trichogramma,size was found to be positively correlated with the number of oocytes at emergence, progeny produced over 24h, searching activity, host and female encounter rates for females and males respectively (Boldt 1974, Bai et al 1992, Kazmer & Luck 1995, Boivin & Lagacé 1999).

Longevity is critical for egg parasitoids especially when it comes to fi nding host patches. Most egg parasitoids are poor

disperser and meteorological conditions such as wind, rain or solar radiation infl uence the capacity of these organisms to disperse to fi nd hosts (Fournier & Boivin 2000, Fatouros et al 2008). Some species even respond to changes in barometric pressure by decreasing their propensity to fl y (Fournier et al 2005). Individuals with a longer life expectancy can survive unfavorable conditions and fi nd hosts afterward. The life expectancy of an individual also modifi es its patch exploitation strategy (Wajnberg et al 2006).

Fecundity is probably the most important fi tness proxy for female egg parasitoids. In numerous egg parasitoid species, a single host egg mass may be suffi cient for a female to deposit all her egg load and a reduced fecundity will translate in lost opportunities and therefore decreased fi tness. The temporal distribution of investment in reproduction in female parasitoids is described by the ovigeny index (Jervis et al 2001). Pro-ovigenic species have all their egg complement mature upon emergence, while synovigenic species have no mature egg at emergence and mature them during their life. Most species of egg parasitoids are either pro-ovigenic or moderately synovigenic, and a large proportion of the potential fecundity of a female is present at emergence (Jervis et al 2001). The potential fecundity at emergence is therefore a good fi tness proxy for these species.

Mating ability is the most important proxy for male egg parasitoids. The sex ratio at the emergence patch is normally strongly females-biased and the males have access to numerous females soon after emergence. The reproduction investment in male parasitoids is described by the spermatogenic index (Boivin et al 2005). Males of Trichogramma species are prospermatogenic (Boivin et al 2005, Damiens & Boivin 2005), males emerge with their full sperm complement and do not produce more in their adult life. In the Mymaridae Anaphes victus Huber, males are moderately synspermatogenic, having an ovigeny index of 0.27 (G Boivin, unpublished data). In species with prospermatogenic males, any increase in the number of sperm present at emergence could enable the male to mate more females if they are present, either on the emergence patch or on another patch.

Vagility is important both for males and females. In males, since off-patch mating occurs (Martel & Boivin 2007), the capacity to disperse to another patch containing females is essential once all females on the emergence patch have been inseminated. Any increase in sperm production could only be expressed if the male has the capacity to disperse. For females, vagility infl uences their capacity to disperse in search of hosts (Bourchier & Smith 1996, Bennett & Hoffmann 1998, Romeis et al 2005). Factors such as wing size and shape infl uence the capacity of Trichogramma females to disperse and therefore affect directly their fi tness through their capacity to fi nd and parasitize hosts (Kölliker-Ott et al 2003).

Phenotypic Plasticity

leave more progeny and therefore gain more fi tness. This selection acts on the genotypic variability that is observed for the proxies within a population. Several studies have looked at genetic variation in life history and behavioral traits of parasitoids (Carton et al 1989, Cronin & Strong 1996). For example, a female with a better vagility will have more chances of fi nding hosts and will be able to express her full potential fecundity (Kölliker-Ott et al 2003, 2004).

Another factor acts on the fi tness proxies. Within a genotype, phenotypic plasticity occurs when the expression of a trait changes with the environment in which the organism is raised (Roff 1992). Phenotypic plasticity is thus the ability of a genotype to produce distinct phenotypes by altering its physiology, morphology, or development in response to changes in the environment (Pigliucci 2005, Colinet et al 2007). Thus, within the same genotype, different individuals will show fi tness proxies that differ based on the conditions under which they developed. Selection will act on the genotype via the expressed phenotype and in a sense will act on the choices made by a female when allocating its progeny to different hosts or habitats. A genotype that expresses phenotypic plasticity in response to external conditions is therefore expected to have a selective advantage in a given condition (Zhivotovsky et al 1996, Moreno-Garcia et al 2010).

Phenotypic plasticity is a major factor in insect parasitoids. For example, the size of adult parasitoids depends on the quality of the host in or on which they developed (Godfray 1994). Siblings that develop in different hosts may express phenotypes that are very different. We will see later which factors infl uence host quality and therefore the expressed phenotype of the adult parasitoid. Such phenotypic plasticity has been demonstrated in several species of egg parasitoids (Olson & Andow 2002) and we expect the fi tness of egg parasitoids to be strongly infl uenced by the factors acting on the phenotypic plasticity.

In egg parasitoids, data support the presence of phenotypic plasticity in morphological and physiological characteristics along with aspects of behavior.

Morphology: size. Size is the most obvious effect of phenotypic plasticity on egg parasitoids. Adults vary in their size based on the host species in which they developed from, the level of superparasitism and factors such as age of the host egg at the time of oviposition. Variation can reach 32-fold in the Pteromalidae Nasonia vitripennis (Walker) (O’Neill & Skinner 1990). Wing length can vary by 36% in the Mymaridae Anaphes nitens Girault when reared on eggs of the snout beetle Gonipterus scutellatus Gyll. (Santolamazza-Carbone et al 2007) and tibia length decreases by 13% in A. victus when females superparasitize host eggs parasitized seven days before (van Baaren et al 1995a).In Trichogramma euproctidis (Girault), female tibia length is 115 μm when they emerge singly from Plutella xylostella (L.), but increases to 196 μm when emerging singly from Trichoplusia ni (Hubner) eggs (V. Martel & G. Boivin, unpublished data). In general, variations in size due to host quality are positively correlated with other fi tness proxies as mentioned before. However, when size differences originate from development at different temperatures, the relationship may be inversely correlated (see

section on duration of development).

Physiology: rate of development. Little information is available on the phenotypic plasticity of duration of development in egg parasitoids. Duration of development is obviously dependent on temperature, but even at the same temperature, the host species could infl uence the duration of the immature stage of egg parasitoids. In T. euproctidis, females that develop in eggs of Plutella xylostella emerge in average after 10.0 days when reared at 24˚C, while females that develop singly in the larger eggs of T. ni emerge in average after 9.4 days (G. Boivin, unpublished data).

Physiology: fecundity of females. Fecundity in most insects varies with body size (Honek 1993) and, as expected, the size of female egg parasitoids has a positive effect on the number of oocytes (O’Neill & Skinner 1990). Lifetime fecundity has been reported to vary from 18 to 56 eggs in females of T. euproctidis that emerged from P. xylostella (head width 140 μm) and Anagasta kuehniella (Zeller) (head width 166 μm), respectively (Boivin & Lagacé 1999). In Trichogramma brassicae Bezdenko, T. evanescens Westwood and T. cacoeciae Marchal, lifetime fecundity increased by 25-30% when reared on A. kuehniella rather than in the smaller eggs of Cadra cautella (Walker) (Özder & Kara 2010). The effect of this parameter is likely to infl uence the number of progeny a female can have and therefore it will infl uence the selection occurring on the associated genotype. A positive correlation between body size and egg size has been reported in Trichogramma species (Klomp & Teerink 1966, G. Boivin unpublished data).

Physiology: number of sperm in males. An equivalent effect of size on the number of sperm in males is described (Henter 2004), but is not universal (Burton-Chellew et al 2007). In general large males have more sperm available on emergence than small males. This reduction in the number of sperm is defi nitive in prospermatogenic species whose males do not produce sperm during their adult live (Boivin et al 2005). However, even in partially synspermatogenic species, where males produce sperm during their adult life, small size could result in fewer sperm that can be stored in the seminal vesicles (Lacoume et al 2006). Obviously males that are limited in the number of sperm available will inseminate fewer females or only partially inseminate females they mate. This limitation will have an effect only in situation where mating opportunities exceed the sperm capacity of males. We expect such situation to occur as a proportion of T. euproctidis males, a prospermatogenic species (Damiens & Boivin 2005), that disperse from the emergence patch after mating is sperm-depleted (Martel & Boivin 2007).

Behavior: patch exploitation. Patch exploitation by female parasitoids integrates several behavioral mechanisms (Pierre et al 2003, Wajnberg 2006) and is also expected to show phenotypic plasticity. Size, through variation in vagility, walking speed, egg load etc.., should influence both the duration of patch exploitation and the number of hosts parasitized. In Aphidius rhopalosiphi De Stefani Perez, smaller females that developed at higher temperature showed a longer patch residence time than larger females (Le Lann 2009). In Trichogramma nubilale Ertle & Davis phenotypic plasticity was found for both percentage parasitism of European corn borer masses and secondary sex ratios (Olson & Andow 2002).

Factors Infl uencing Phenotypic Variability in Egg Parasitoids

Host species. Parasitoids show some phenotypic plasticity in their host choice (Vos & Vet 2004). Obviously, the size of the host in which an egg parasitoid develops infl uences the size of the emerging adult and therefore several of its life history traits including host fi delity (Henry et al 2010). The quality of the host could also infl uence the size of the emerging adult. Two host eggs of the same size but from different species could represent resources of different nutritive values. This factor is likely to be more important in generalist species exploiting different host species.

Host condition. The size of the host is not the only factor that could infl uence the fi tness of the developing parasitoid. As the host embryo develops within the egg, resources are used and although egg parasitoids can recycle part of the transformed resources, some of it is lost. As a result, egg parasitoid immatures that develop in older eggs have fewer resources to use and old host eggs are generally less preferred by most Trichogrammatidae species (Godin & Boivin 2000). However, because the size of the host egg does not change markedly as it ages, adults emerging from old and young host eggs show only a 15% difference in size, but females emerging from old host eggs show a reduction in fecundity of 80% (G. Boivin, unpublished data).

Other factors acting on host egg quality could also influence the phenotypic plasticity of the developing parasitoid, but few data is available to support this (Jervis et al 2008). The quality of the food of the host adult is expected to modify the quality of the egg content and indirectly act on the developing egg parasitoid. When the Scelionidae Telenomus podisi Ashmead developed in eggs of the predatory pentatomid Podisus maculiventris (Say) that fed on caterpillar that developed on herbivore-resistant soybean, its overall reproductive capacities was negatively affected (Orr & Boethel 1986).

Duration of development. The phenotypic plasticity of egg parasitoid could also be infl uenced by the duration of their development. As in most poikilotherm species, duration of development is infl uenced by temperature, individuals developing at higher temperature develop faster than at low temperature. The rate of development infl uences the size of the

adult according to the Temperature-Size Rule (TSR) (Atkinson 1994, Angilletta et al 2004). The longer the development, the larger will be the adult at the end of its development. The TSR has been verifi ed in several parasitoid species (Elliott et al 1995, Bazzocchi et al 2003, Colinet et al 2007) and the rate of development infl uenced negatively not only size, but also fecundity, lipid reserve and longevity (Colinet et al 2007). The mechanism behind the TSR is still debated (Angilletta et al 2004), the individuals developing at low temperature could grow larger either because they have access to resources for longer or their use of the resources could be more effi cient at low temperature.

The application of TSR to idiobiont parasitoids, such as egg parasitoids, is more problematic. Once an egg parasitoid immature is within its host egg, the resources are fi xed and the size of the egg chorion does not change. Nonetheless, in preliminary tests, we showed that T. euproctidis reared at 15°C were signifi cantly larger than when reared at 30°C as predicted by the TSR (G. Boivin unpublished data). However, the other parameters measured showed the opposite trend. The adults reared at 30°C, even if smaller, had a longer lifespan and the females were more fecund. Because the resources were fi xed, the increase in size found in individuals reared at low temperature could be compensated by a decrease in reserve that refl ected in longevity and fecundity. On the other hand, selection experiments showed that over 15 generations, the temperature at which oviposition occurred changed the effi ciency of female Trichogramma pretiosum Riley at low and high temperatures (Carrière & Boivin 2001).

These data on TSR on egg parasitoids stress the fact that a positive correlation between size and other life history traits should not be taken as granted.

Competition. In solitary species, when two or more larvae share a host, contest competition occurs and supplementary larvae are killed either by direct fi ght or through physiological suppression (Mackauer 1990, Carignan et al 1995). Superparasitism is generally avoided through host discrimination (Roitberg & Mangel 1988), a behavior not unique to Hymenoptera parasitoids (Royer et al 1999). In gregarious and facultative gregarious parasitoid species, resources within a host have to be shared through scramble competition. The less resources available per developing immature, the smaller will be the adults emerging from that host (van Baaren et al 1995b). Immatures of Trichogramma feed very rapidly at the beginning of their development and most of the host egg resources are consumed within 9h after hatching at 25°C (Wu et al 2000). When several Trichogramma larvae share a host egg, some will be consumed by other larvae while the others will reach the pupal stage. Depending of the outcome of the scramble competition, the size of the emerging Trichogramma can be quite variable (G. Boivin unpublished data).

Nagaraja females (Ahmad et al 2002) while the hind tibia length of T. evanescens varied from 192 μm for solitary individuals to 142 μm (four individuals per host egg) in eggs of Mamestra brassicae (L.) (Grenier et al 2001). There is generally a positive relationship between the size of the adults and most of the other fi tness proxies measured when the difference in size is caused by competition within the host egg.

Conclusion

Measuring fi tness in egg parasitoids is important both in behavioral ecology and biological control studies. The value of an individual can vary tremendously within the same genotype and this phenotypic plasticity has to be taken into account when evaluating behavioral choices or the effi ciency of egg parasitoids to control a pest population. While size is often used to assess the value of individuals, the use of this proxy can be misleading.

When the variability in size is caused by intraspecifi c competition within the host egg, a positive relationship is found between the size of the adult and its reproductive capacity. The slope of the relationship changes when the difference in size is due to the quality of the host egg. Females developing in old host eggs are only 15% smaller than those developing in young host eggs yet their fecundity is decreased by 85%. When the difference in size is due to difference in rearing temperature, the effect can even be reversed, larger individuals that developed at lower temperature show a lower fecundity and longevity than smaller individuals reared at higher temperature. The safest solution remains the measure of several fi tness proxies to provide a true picture of the value of an individual.

Acknowledgments

This research was supported in part by a grant from the Natural Sciences and Engineering Research Council of Canada (NSERC).

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